FDA UDI Not in Commercial Distribution 🇺🇸 United States

N/A

DI: 00885556606247 · Model: 3766F · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
N/A
Primary DI
00885556606247
Version / Model
3766F
Catalog Number
3766F
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-22
Public Version
6
Public Version Date
2023-11-17
Public Version Status
Update
Public Device Record Key
777a8c4f-36a9-40d8-9012-fbb74ce5e86b
Distribution End Date
2021-02-12

Device Description

RFB.VAS POST TWD DOV EG 4 MMX30DEG

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HRX ARTHROSCOPE

GMDN Terms

Code Name
34856 Rigid optical arthroscope, reusable

Identifiers

Type ID
Primary 00885556606247

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K971253 000